基于单光纤OCT的球形眼模型实时估计研究

P. Cornelissen, M. Ourak, G. Borghesan, D. Reynaerts, E. V. Poorten
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引用次数: 2

摘要

深度感知仍然是玻璃体视网膜手术的关键挑战。目前,用户只能从头顶的立体显微镜上看到,但这种可视化手段是相当有限的。光学相干层析成像(OCT)在过去已经被引入,甚至被集成到许多商业系统中,以提供更详细的深度视觉,甚至可以显示地表以下几毫米的地下结构。术中OCT的使用,特别是与机器人技术的结合,仍然是次优的。目前,人们可以得到更新非常缓慢的大容量扫描(c扫描)或更快但不对齐的横断面b扫描或更局部的单点a扫描,更新率非常高。在这项工作中,我们提出了一种模型介导的方法。由于眼后段可以近似为一个球体,我们提出用这个简化的球体模型对视网膜进行建模,可以实时估计其中心和半径。本文提出了一种时变卡尔曼滤波器与仪器集成光纤相结合,该光纤可沿仪器纵向方向提供高频A扫描。模型和模型的收敛性首先在仿真环境中进行了验证,随后使用安装在协同操作的玻璃体视网膜机器人系统上的OCT a扫描探针进行了计算机验证。该探针被用来测量眼后段的三维立体光刻球形模型。在各种场景下验证了该方法的可行性。对于计算机验证,当采样频率为200Hz时,发现误差为20微米,收敛速度为2.0秒。
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Towards Real-time Estimation of a Spherical Eye Model based on a Single Fiber OCT
Depth perception remains a key challenge in vitreoretinal surgery. Currently users only have the view from an overhead stereo-microscope available, but this means of visualisation is quite restrictive. Optical Coherence Tomography (OCT) has been introduced in the past and is even integrated in a number of commercial systems to provide a more detailed depth vision, even showing subsurface structures up to a few millimeters below the surface. The intra-operative use of OCT, especially in combination with robotics, is still sub-optimal. At present one can get either a very slowly updating large volume scan (C-scan) or a faster but not aligned cross-sectional B-scan or an even more local single point A-scan at very high update rate. In this work we propose a model-mediated approach. As the posterior eye segment can be approximated as a sphere, we propose to model the retina with this simplified sphere model, the center and radius of which can be estimated in real time. A time-varying Kalman filter is proposed here in combination with an instrument-integrated optical fiber that provides high-frequency A-scans along the longitudinal instrument direction. The model and convergence of the model has been validated first in a simulation environment and subsequently in-silico using an OCT A-scan probe mounted on a co-manipulated vitreoretinal robotic system. The probe was manipulated to measure a 3D stereo lithographically printed spherical model of the posterior eye segment. The feasibility of the proposed method was demonstrated in various scenarios. For the in-silico validation a 20 micrometer error and convergence speed of 2.0 seconds was found when sampling A-scans at 200Hz.
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